Minimally Invasive Cardiac Output Monitoring Device
Completed · Not applicable
Conditions studied: Cardiac Event
In brief
The overall goal of this collaborative study is to advance the novel "pulse contour analysis" to the point at which it can be incorporated into a real-time device. The specific objective is to establish an auto-calibration algorithm that conveniently yields cardiac output (CO) in units of liters-per-minute. To achieve this objective, the waveforms for analysis and reference pulmonary artery catheter CO measurements will be recorded from critically ill patients and then analyzed off-line at Retia Medical. Successful completion of this study may ultimately help lead to improved outcomes of critically ill patients.
Key facts
- Study ID
- NCT01675063
- Run by
- University of Michigan
- People needed
- 77
- Starts
- 2012-08-01
- Expected to finish
- 2015-10-01
- Last updated by the study team
- 2017-05-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All adult patients admitted to the University of Michigan ICU following cardiac surgery with both a pulmonary and radial artery catheter.
You may not qualify if…
- Adult patients with mechanical cardiac support including intra-aortic balloon pumps, LVAD, or ECMO, and persistent ventricular arrhythmias.
Where it is running
- University of Michigan — Ann Arbor, Michigan, United States
Full record on ClinicalTrials.gov
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